Terrasil Itch, Rash And Pain Relief
FDA Label NDC 24909-154

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Aidance Skincare & Topical Solutions, Llc for the product Terrasil Itch, Rash And Pain Relief (NDC 24909-154). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, keep out of reach of children., directions, inactive ingredients, principal display panel - 44g label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Allantoin 0.5%, Menthol 0.15%

Purpose

Allantoin - Skin Protectant

Menthol - Topical Anesthetic

Uses

For temporary protection and relief of pain and itching associated with minor skin irritations, rashes, eczema and/or insect bites.

Warnings

For external use only. Avoid contact with eyes. Do not apply to open wounds
or damaged skin. If symptoms persist for more than seven days, discontinue use and
consult physician. If swallowed, consult physician. Do not bandage tightly.
If pregnant or breast feeding, contact physician prior to use.

Keep Out Of Reach Of Children.

If swallowed, consult physician.

Directions

Apply directly to effected area. Do not use more than four
times per day. Store at room temperature.

Inactive Ingredients

bentonite, cera alba (organic beeswax), cotton seed oil, eucalyptus citriodora oil, magnesium oxide, peppermint oil, silver oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide.

Principal Display Panel - 44G Label

Jar Label (Terrasil Irp Max Label 44g 050815)

Jar Label (Terrasil Irp Max Label 44g 050815)

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